Lack of the bone morphogenetic protein BMP6 induces massive iron overload (Q28510138)

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English	Lack of the bone morphogenetic protein BMP6 induces massive iron overload	scientific journal article

Statements

instance of

scholarly article

1 reference

stated in

PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

title

Lack of the bone morphogenetic protein BMP6 induces massive iron overload (English)

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stated in

PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

main subject

Solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2

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GOA release 2020-03-11

Solute carrier family 40 (iron-regulated transporter), member 1

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GOA release 2020-03-11

SMAD family member 1

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GOA release 2020-03-11

SMAD family member 9

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GOA release 2020-03-11

Bone morphogenetic protein 6

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GOA release 2020-03-11

SMAD family member 5

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GOA release 2020-03-11

morphogenesis

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based on heuristic

inferred from title

iron

1 reference

based on heuristic

inferred from title

iron overload

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inferred from title

author

Léon Kautz

object named as

Léon Kautz

series ordinal

2

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François Canonne-Hergaux

object named as

François Canonne-Hergaux

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4

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author name string

Delphine Meynard

series ordinal

1

1 reference

stated in

PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

Valérie Darnaud

series ordinal

3

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PubMed

PubMed publication ID

19252488

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24 January 2017

Hélène Coppin

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5

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PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

Marie-Paule Roth

series ordinal

6

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PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

language of work or name

English

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publication date

1 April 2009

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stated in

PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

published in

Nature Genetics

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stated in

PubMed

PubMed publication ID

19252488

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24 January 2017

volume

41

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PubMed

PubMed publication ID

19252488

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24 January 2017

issue

4

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PubMed

PubMed publication ID

19252488

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24 January 2017

page(s)

478–481

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PubMed

PubMed publication ID

19252488

retrieved

24 January 2017

cites work

Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Bone morphogenetic proteins 2, 4, and 9 stimulate murine hepcidin 1 expression independently of Hfe, transferrin receptor 2 (Tfr2), and IL-6

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Iron regulates phosphorylation of Smad1/5/8 and gene expression of Bmp6, Smad7, Id1, and Atoh8 in the mouse liver

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

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21 April 2017

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

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21 April 2017

Mechanisms of TGF-beta signaling from cell membrane to the nucleus

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

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21 April 2017

A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

A mouse model of juvenile hemochromatosis

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Targeted disruption of the hepcidin 1 gene results in severe hemochromatosis

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

The family of bone morphogenetic proteins

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Presence of the iron exporter ferroportin at the plasma membrane of macrophages is enhanced by iron loading and down-regulated by hepcidin

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Relative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

A new mathematical model for relative quantification in real-time RT-PCR

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.320

retrieved

21 April 2017

Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.320

retrieved

21 April 2017

Hepcidin is decreased in TFR2 hemochromatosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the DMT1 (NRAMP2/DCT1) iron transporter in mice with genetic iron overload disorders.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

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inferred from PubMed ID database lookup

A bone morphogenetic protein (BMP)-responsive element in the hepcidin promoter controls HFE2-mediated hepatic hepcidin expression and its response to IL-6 in cultured cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemochromatosis--neonatal and young subjects

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactivation of the hemochromatosis gene differentially regulates duodenal expression of iron-related mRNAs between mouse strains

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mice lacking Bmp6 function

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone morphogenetic proteins and their antagonists

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19252488

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NG.320

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2175250

OpenCitations bibliographic resource ID

2175250

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2175250

PubMed publication ID

19252488

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2175250

ResearchGate publication ID

24147017

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